510(k) K242748

Device
Oncospace
Applicant
Oncospace, Inc.
510(k) number
K242748
Product code
MUJ
Decision
Substantially Equivalent (SESE)
Decision date
2025-04-11
Date received
2024-09-12
Regulation
892.5050
Classification name
System, Planning, Radiation Therapy Treatment
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Sigrid Schoepel
Address
1812 Ashland Ave., Suite 100k Baltimore MD US 21205 21205

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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